Welcome to SNPscan. Your input file should be a text output file exported from Affymetrix's Copy Number Analysis Tool (CNAT) v2.0 or later, with the first line ("Copy Number Analysis Tool" form CNAT 2.0/2.1 or "Copy Number Viewer" from CNAT 3.0) been deleted. If you use CNAT 3.0 or GTYPE 4.0, do not use any file saved in the ".cnt" file format as your input to SNPscan. Select "Export", "Table" form Copy Number Viewer's menu bar to save you SNP data as a tab-delimited file. The first line of your input file shall be ColumnNanes (column headers), followed by Data lines, one line per SNP. The first field of each Data lines shall be a serial number for that SNP. SNPscan expects the ColumnNames to be in the exact format exported by the Copy Number Analysis Tool (XXX_Call, XXX_SPA_CN, etc.) Visit the sample data page to see examples of the appropriate formats.
The current file size limitation is 40 MB per upload. It's enough for 10 100K SNP cases. You can increase this limitation by installing SNPscan locally (instructions).
The Copy Number of each SNP will be plotted as dots against chromosomal positions, color coded according to each SNP's call: AA, BB, AB, NoCall. In addition, LOH and p-value can also be plotted, as gray bars and yellow lines, respectively.
Sample SNPscan Plot Patterns:
Normal Autosomes
Duplication
Normal Female Chromosome X
Uniparental Isodisomy
Normal Male Chromosome X
Hemizygous Deletion (High LOH, high p_value, some dots below 1)
Mosaic Female Chromosome X
Mosaic Microdeletion (Low LOH, low p_value, very few dots below 1)